Small paeds topics Flashcards

1
Q

What are the two most common severe inherited coagulation disorders?

A

Haemophilia A

Haemophilia B

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What type of inhertiance are haemophilias?

A

X linked recessive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Which is more common haemophilia A or B?

A

A - 5x more common

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the cause of haemophilia a?

A

Defective synthesis of VIII

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the main symptom of haemophilia?

A

BLEEDING

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is bleeding into muscles called?

A

Haemarthroses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What clotting time will be longer in haeophilia a/b?

A

APTT

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the management for haemophilia a/b?

A

Give the factor they are short of
A=8
B=9

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the complication of giving clotting factors as treatment?

A

Antibodies to factors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Which drug can be used to treat mild haemophilia A?

A

Desmopressin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is the cause haemophilia b?

A

Deficiency of clotting factor 9

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is VWF disease?

A

VWF factor (released by activated thrombin) preents degradation of factor 8 complex from degradation. Decreased VWF = decreased clotting ability

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the standard treatment of children with IDA?

A

5mg/kg/day of ferrous suplhate + vitamin C (improves absortption)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What type of anaemia do you get in IDA?

A

Microcytic anaemia
Hypochromic
low MCV
low MCH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What happens to reticulocytes in IDA?

A

Decreased (rise in a few days of treatment)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What investigation would show you sickle cell disease?

A

Blood film

17
Q

What investigation would show G6PD deficiency and pyruvate kinase deficiency?

A

Red cell enzyme studies

18
Q

When do most children become symptomatic in IDA?

A

Hb drops below 70g/L

19
Q

What investigation would you nee to do to diagnose a thallasaemia?

A

Haemoglobin electrophoresis

20
Q

Explain how Iron deficiency leads to anaemia?

A

Decreased production of red blood cells due to ineffective erythropoiesis

21
Q

Main 3 causes for IDA?

A

Inadequate intake
Malabsorption
Blood loss

22
Q

What type of anaemia does thalassaemia cause?

A

Microcytic

23
Q

What type of anaemia does thalassaemia cause?

A

Microcytic

24
Q

What are the different severity of B thalassamia?

A

All affected individuals a have a severe reduction in B globin

B major - HbA (a2b2) cannot be made because abnormal B globin gene

B intermdia - B globin mutation allows a small amount of HbA and/or HbF to be produced

25
Q

What happens as the result B thalassaemia?

A

1) Severe anaemia within 3/12 (transfusion dependent)
2) Extra medullary haemopoeisis (prevented by regular blood transfusions) –> patinets develop hepatosplenomegaly and bone marrow explansion
3) bone marrow expansion can lead to maxillary overgrowth and skull bossing

26
Q

What chrmosome is affected for thalassaemia B?

A

11

27
Q

What is the treatment for B thalassaemia?

A

Transfusions life long (Bone marrow transplant - cure, need a HLA identical sibling)

28
Q

What are the complications with transfusions for B thaassameia?

A

1) IRON DEPOSITION
2) antibody formation - 10% - aallo-antibodies to transfused red cells in the patient make finding compatible blood difficult
3) venous access

29
Q

What is a ‘cure treatment’ for B thalassaemia?

A

Bone marrow transplantation

30
Q

Can you test prenatally for B thalassaemia?

A

Yes in CVS - for at risk people

31
Q

Who is sickle cell disease more common in?

A

African and carribean

32
Q

What is sickle cell disease?

A

You get HbS instead of HbA. This makes the RBC sickle shaped

33
Q

What is sickle cell trait?

A

one HbS from one patent and one normal B globin gene

34
Q

What are the features of sickle cells?

A

Low life span
Can be trapped in the microcirculation resulting in blood vessel occlusion and thus iscahemia in an organ or bone (the trapping is exacerbated by low oxygen tension, dehydration and cold)

35
Q

How do homozygotes present?

A

Recurrent episodes of haemolysis crises (from infancy)

36
Q

What organisms do sickle cell sufferers have an increased susceptibility to?

A

Encapsulated organisms - pneumococci and haemophilus influenzae

Also increased of incidence of osteomyelitis caused by salmonella and otehr organisms